REDPINE

GUDID 06972520300943

Guangzhou Red Pine Medical Instrument Co., Ltd.

Rigid endoscopic biopsy forceps, single-use Rigid endoscopic biopsy forceps, single-use

• Primary Device ID: 06972520300943
• NIH Device Record Key: 3a45a72f-c2a7-4fff-a5ac-224d9178f1d4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: REDPINE
• Version Model Number: RP-U-P1502
• Company DUNS: 417649868
• Company Name: Guangzhou Red Pine Medical Instrument Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06972520300943 [Primary]

FDA Product Code

• FCL: Forceps, Biopsy, Non-Electric

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-09-04
• Device Publish Date: 2023-08-25

On-Brand Devices [REDPINE]

• 06972520300943: RP-U-P1502
• 06972520300936: RP-IPD-V800
• 06972520300912: RP-U-C0305S3
• 06972520300905: RP-U-C0305S9
• 06972520300899: RP-U-C0305R3
• 06972520300882: RP-U-C0305
• 06972520300875: RP-U-C0304S3
• 06972520300868: RP-U-C0304S9
• 06972520300851: RP-U-C0304R3
• 06972520300844: RP-U-C0304
• 06972520300837: RP-U-C12S3
• 06972520300820: RP-U-C12S9
• 06972520300813: RP-U-C12R3
• 06972520300806: RP-U-C12
• 06972520300776: RP-U-P1101
• 06972520300769: RP-U-P1302
• 06972520300752: RP-U-P0901
• 06972520300134: RP-U-C0305
• 06972520300066: RP-IPD-V800
• 06972520300011: RP-U-C12